Canonical Allele Identifier: PA2827783514
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Arg1568Cys
CA145250
NM_001353957.2:c.4702C>T